Variant #0000525825 (NC_000005.9:g.52954436T>G, NM_002495.2:c.406T>G (NDUFS4))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52954436T>G
DNA change (hg38) g.53658606T>G
Published as NDUFS4(NM_002495.2):c.406T>G (p.(Ser136Ala)), NDUFS4(NM_002495.3):c.406T>G (p.S136A)
ISCN -
DB-ID NDUFS4_000008 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS4 NM_002495.2 -?/. - c.406T>G r.(?) p.(Ser136Ala)


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